2020
DOI: 10.14309/01.ajg.0000712920.97943.a8
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S2718 Harmful Gains: Drug-Induced Liver Injury From Selective Androgen Receptor Modulators

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Cited by 4 publications
(14 citation statements)
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“…As a result, they can have similar outcomes as AASs, resulting in three types of liver injury due to augmented cell growth, which include hepatic tumors, peliosis hepatis, and nodular regenerative hyperplasia. Due to the increase in the use of SARMs, it is essential to report these cases as early as possible to help recognize the offending agent and to understand its long-term effects [6].…”
Section: Discussionmentioning
confidence: 99%
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“…As a result, they can have similar outcomes as AASs, resulting in three types of liver injury due to augmented cell growth, which include hepatic tumors, peliosis hepatis, and nodular regenerative hyperplasia. Due to the increase in the use of SARMs, it is essential to report these cases as early as possible to help recognize the offending agent and to understand its long-term effects [6].…”
Section: Discussionmentioning
confidence: 99%
“…Unlike AASs, which have both anabolic and androgenic properties, SARMs express positive effects on muscles and bones without causing any androgenic effects of AASs. Due to these favorable properties, they are also marketed by some supplement manufacturers as legal steroids and also being desiccated for the management of osteoporosis, cachexia, and sarcopenia [4][5][6]. Although FDA and world anti-doping agency have not approved the use of SARMs, they are very popular among athletes and are heavily promoted as AAS alternatives [3,5].…”
Section: Introductionmentioning
confidence: 99%
“…Aside from bodybuilding supplements, the men were not using other medications except for one who was on venlafaxine and another who was on zopiclone and finasteride. 14,15,18,20,21,28,29,37,67,68 The demographics of patients with DILI from SARMs were highly consistent with the demographics of DILI from AAS. From 1994 to 2013, all cases of DILI from AAS in the Spanish DILI Registry and Latin DILI Network were in men from 20 to 49 years of age with a mean of 32 years.…”
Section: Epidemiologymentioning
confidence: 53%
“…Latency period in idiosyncratic injury can vary as was seen in a number of SARM-related DILI cases in which the time to symptoms onset ranged from approximately 4 to 12 weeks. [27][28][29] Outside of the acute cholestatic syndrome, clinical trials have shown that SARMS have the potential to induce transient liver enzyme elevations that have resolved without discontinuation of the drug. 30,31 17α-alkylated AASs have also been linked to transient serum elevations that resolve without discontinuation.…”
Section: Hepatotoxicitymentioning
confidence: 99%
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